Literature DB >> 33977474

Active GTPase Pulldown Protocol.

Martin J Baker1, Ignacio Rubio2,3.   

Abstract

Ras and its related small GTPases are important signalling nodes that regulate a wide variety of cellular functions. The active form of these proteins exists in a transient GTP bound state that mediates downstream signalling events. The dysregulation of these GTPases has been associated with the progression of multiple diseases, most prominently cancer and developmental syndromes known as Rasopathies. Determining the activation state of Ras and its relatives has hence been of paramount importance for the investigation of the biochemical functions of small GTPases in the cellular signal transduction network. This chapter describes the most broadly employed approach for the rapid, label-free qualitative and semi-quantitative determination of the Ras GTPase activation state, which can readily be adapted to the analysis of other related GTPases. The method relies on the affinity-based isolation of the active GTP-bound fraction of Ras in cellular extracts, followed by its visualization via western blotting. Specifically, we describe the production of the recombinant affinity probes or baits that bind to the respective active GTPases and the pulldown method for isolating the active GTPase fraction from adherent or non-adherent cells. This method allows for the reproducible measurement of active Ras or Ras family GTPases in a wide variety of cellular contexts.

Entities:  

Keywords:  Activation; Arf; Cdc42; GTPase; Pulldown; RBD; Rab; Rac; Ral; Ran; Rap; Ras; Rho; Rin/Rit

Year:  2021        PMID: 33977474     DOI: 10.1007/978-1-0716-1190-6_7

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  49 in total

1.  Quantification of absolute Ras-GDP/GTP levels by HPLC separation of Ras-bound [(32)P]-labelled nucleotides.

Authors:  Ignacio Rubio; Rico Pusch; Reinhard Wetzker
Journal:  J Biochem Biophys Methods       Date:  2004-02-27

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Journal:  Nature       Date:  1990-08-23       Impact factor: 49.962

3.  Ras history: The saga continues.

Authors:  Adrienne D Cox; Channing J Der
Journal:  Small GTPases       Date:  2010-07

4.  Determination of guanine nucleotides bound to Ras in mammalian cells.

Authors:  J B Gibbs
Journal:  Methods Enzymol       Date:  1995       Impact factor: 1.600

5.  Measurements of GTP/GDP exchange in permeabilized fibroblasts.

Authors:  A M de Vries-Smits; J Downward; J L Bos
Journal:  Methods Enzymol       Date:  1995       Impact factor: 1.600

6.  Determination of absolute amounts of GDP and GTP bound to Ras in mammalian cells: comparison of parental and Ras-overproducing NIH 3T3 fibroblasts.

Authors:  J S Scheele; J M Rhee; G R Boss
Journal:  Proc Natl Acad Sci U S A       Date:  1995-02-14       Impact factor: 11.205

7.  Rnd proteins: multifunctional regulators of the cytoskeleton and cell cycle progression.

Authors:  Philippe Riou; Priam Villalonga; Anne J Ridley
Journal:  Bioessays       Date:  2010-09-10       Impact factor: 4.345

8.  Guanine nucleotide-binding activity as an assay for src protein of rat-derived murine sarcoma viruses.

Authors:  E M Scolnick; A G Papageorge; T Y Shih
Journal:  Proc Natl Acad Sci U S A       Date:  1979-10       Impact factor: 11.205

9.  Ras activation in response to lysophosphatidic acid requires a permissive input from the epidermal growth factor receptor.

Authors:  Ignacio Rubio; Knut Rennert; Ute Wittig; Reinhard Wetzker
Journal:  Biochem J       Date:  2003-12-15       Impact factor: 3.857

10.  Phosphorylated Rho-GDP directly activates mTORC2 kinase towards AKT through dimerization with Ras-GTP to regulate cell migration.

Authors:  Hiroshi Senoo; Yoichiro Kamimura; Reona Kimura; Akihiko Nakajima; Satoshi Sawai; Hiromi Sesaki; Miho Iijima
Journal:  Nat Cell Biol       Date:  2019-07-01       Impact factor: 28.824

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